Evidence map›Paper›PMID 34725261›Full record

ArticleRMD open2021

Contrasting role of

Dan Lévy, Alexandre Mariotte, Aurore DeCauwer, Cecile Macquin, Angélique Pichot, Anne Molitor, Francois Maurier, Alain Meyer, Raphael Carapito, Philippe Georgel

Open access · goldAbstract readCase Reports
In one paragraph

Article in RMD open, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.6field-weighted citation impact, top 32% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Pattern Recognition by NOD-Like Receptors.Advances in experimental medicine and biology · 2025
    Review
  7. RMD open · 2023
    Review
  8. Article
  9. JAAD case reports · 2022
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Dan LévyExplorations Fonctionnelles Musculaires, Service de Physiologie, Hôpitaux Universitaires de Strasbourg, Strasbourg Cedex, Strasbourg, France.
Alexandre MariotteUniversité de Strasbourg, Faculté de Médecine, Strasbourg, France.
Aurore DeCauwerUniversité de Strasbourg, Faculté de Médecine, Strasbourg, France.
Cecile MacquinUniversité de Strasbourg, Faculté de Médecine, Strasbourg, France.
Angélique PichotUniversité de Strasbourg, Faculté de Médecine, Strasbourg, France.
Anne MolitorUniversité de Strasbourg, Faculté de Médecine, Strasbourg, France.
Francois MaurierHôpitaux Privés de Metz, Metz, France.
Alain MeyerExplorations Fonctionnelles Musculaires, Service de Physiologie, Hôpitaux Universitaires de Strasbourg, Strasbourg Cedex, Strasbourg, France.ORCID 0000-0003-0893-6041
Raphael CarapitoUniversité de Strasbourg, Faculté de Médecine, Strasbourg, France.
Philippe GeorgelUniversité de Strasbourg, Faculté de Médecine, Strasbourg, France pgeorgel@unistra.fr.ORCID 0000-0001-6853-7080
Inserm · FRHôpitaux Universitaires de Strasbourg · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo explore at the molecular level the phenotype of a patient suffering an autoinflammatory syndrome which was diagnosed as familial cold autoinflammatory syndrome type 2 (FCAS-2). To explore the functions of Nlrp12 in inflammation using mouse models.

methodsWhole exome sequencing and Nlrp12 targeted resequencing were performed on DNA isolated from the patient and her family members. In vivo and ex vivo models of inflammation (urate crystals-dependent acute joint inflammation and urate crystals-induced peritonitis) were analysed in Nlrp12-deficient and Nlrp12-competent mice.

resultsA rare missense NLRP12 variant (c.857C>T, p.P286L) was identified in the patient and her healthy relatives. Nlrp12-deficient mice exhibit reduced systemic inflammation and neutrophilic infiltration.

conclusionNlrp12 mediates proinflammatory functions in mice. In humans, the identification of Nlrp12 variants must be cautiously interpreted depending on clinical and paraclinical data to diagnose FCAS-2.

Indexed as

ArthritisCryopyrin-Associated Periodic SyndromesAnimalsFemaleHumansIntracellular Signaling Peptides and ProteinsMiceMutation, MissensePhenotypeIntracellular Signaling Peptides and ProteinsNLRP12 protein, humanNLRP12 protein, mouseautoimmune diseasesinflammationrheumatic fever

Identifiers

PMID34725261
PMCPMC8562517
OpenAlexW3210543147

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.